scholarly journals Sclerosing stromal tumor of the ovary presenting as precocious puberty: Unusual presentation of the rare neoplasm

2014 ◽  
Vol 4 (3) ◽  
pp. 307 ◽  
Author(s):  
JaiKumar Chaurasia ◽  
Nishat Afroz ◽  
Veena Maheshwari ◽  
Mohammed Naim
2018 ◽  
Vol 22 (4) ◽  
pp. 375-379 ◽  
Author(s):  
Anthony I Squillaro ◽  
Shengmei Zhou ◽  
Stefanie M Thomas ◽  
Eugene S Kim

Precocious puberty in an infant is an alarming and infrequent finding, making the differential diagnosis difficult for practitioners. Precocious puberty secondary to a sclerosing stromal tumor (SST) of the ovary is rare. We present a case of a child that began precocious puberty at 3 months of age including development of breast buds, pubic hair, growth spurt, and menarche 5 days prior to presenting to pediatric endocrinology at 10 months. She underwent right salpingo-oophorectomy which demonstrated a soft tissue mass occupying almost the entire ovary with a tan-pink fleshy cut surface. Histological examination confirmed a variant of SST. This case represents an extremely young onset of precocious puberty secondary to a variant of SST without hormonal elevation.


2006 ◽  
Vol preprint (2007) ◽  
pp. 1
Author(s):  
Odette Hall ◽  
Judy Pascasio ◽  
Jennifer Morrissette ◽  
Christopher Newton ◽  
Marshall Schwartz ◽  
...  

2014 ◽  
Vol 2014 (mar31 1) ◽  
pp. bcr2013201124-bcr2013201124 ◽  
Author(s):  
J. K. Chaurasia ◽  
N. Afroz ◽  
V. Maheshwari ◽  
M. Naim

2005 ◽  
Vol 18 (8) ◽  
pp. 1121-1126 ◽  
Author(s):  
Brigitte K Nixon ◽  
Steven J Kussick ◽  
Michael J Carlon ◽  
Brian P Rubin

2008 ◽  
Vol 19 (4) ◽  
pp. 270 ◽  
Author(s):  
Hyun Sik Youm ◽  
Dong Soo Cha ◽  
Kyoung Hee Han ◽  
Eun Young Park ◽  
Naomi Nahyoung Hyon ◽  
...  

2020 ◽  
Vol 43 (1) ◽  
pp. 47-49
Author(s):  
B Vidal Vílchez ◽  
A Caballero Mateos ◽  
F Berdugo Hurtado ◽  
A Ortiz Sánchez ◽  
M Valenzuela de Damas

Resumen La presentación del tumor del estroma gastrointestinal (GIST) ileal como un abdomen agudo no es frecuente. Presentamos el caso de un varón de 75 años que debutó en forma de cuadros suboclusivos de repetición y hemorragia digestiva, siendo diagnosticado de GIST ileal mediante cápsula endoscópica. Fue sometido a cirugía con resección de dos segmentos de asa de intestino delgado y múltiples implantes, asociado a terapia adyuvante con Imatinib con posterior recidiva tumoral.


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